Clinical Trials Coordination and Advisory Group
Article 85
1. A Clinical Trials Coordination and Advisory Group (CTAG), composed of the national contact points referred to in Article 83 is hereby established. 2. The CTAG shall have the following tasks: (a) to support the exchange of information between the Member States and the Commission on the experience acquired with regard to the implementation of this Regulation; (b) to assist the Commission in providing the support referred to in the second paragraph of Article 84; (c) to prepare recommendations on criteria regarding the selection of a reporting Member State. 3. The CTAG shall be chaired by a representative of the Commission. 4. The CTAG shall meet at regular intervals and whenever the situation requires, on a request from the Commission or a Member State. Any item of the agenda of the meeting shall be placed at the request of the Commission or a Member State. 5. The secretariat shall be provided by the Commission. 6. The CTAG shall draw up its rules of procedure. The rules of procedure shall be made public.